Service Details:
Minimum Order Quantity | 1 Day |
Range | All Range |
Required Standards | ISO IEC 17025-2017 |
Calibrated For | 1 year |
Usage/Application | Healthcare Industry |
Cleanroom Type | Softwall Cleanroom |
Mode Of Report | Hard Copy |
Validation Type | Fume Exhaust System Testing |
Room Size | <200 Square Feet |
Certification Type | Biosafety Certification |
Instrument Validation | Breathing Air Validation |
Prevention Particle | Dust |
Number Of Rooms | >3 |
Key Instruments | Validation |
Validation is an important process for any cleanroom. It serves to ensure that the cleanroom is properly installed and designed for its intended ISO classification and that all of the components (facility, environment, equipment) meet regulatory requirements and other defined standards.Cleanroom Validation/HVAC Validation is performed for a variety of reasons. To ensure that the design of the facility is fit for its intended purpose; to ensure that the facility, equipment, and environment meets User Requirement Specifications (URS); to ensure that the facility, equipment, and environment meet defined regulatory requirements; to ensure that the facility, equipment, and its environment function together as a system to meet defined standards.
Additional Information:
- Item Code: Validation
- Production Capacity: Cleanroom Validation
- Packaging Details: Service Details:
Validation Type Recovery Test
Cleanroom Type Modular Cleanroom
Application/Usage Lab
Room Size >500 Square Feet
Prevention Particle Dust
Instrument Validation Laminar Air Flow Validation
AMC Required Yes
Key Instruments Anemometer, Particle counter, Fogger, Photometer, Generator
Testings are carried out in accordance with relevant standards (ISO 14644-2, 3, 4, EU GMP/EC GMP, FS 209E, WHO 2002, USFDA, MHRA, Drug and Cosmetic Act of India, 2005)
We carried following services in validation, 1. Air Velocity (Flow) Test ACPH test ,2. HEPA filter integrity Test, 3. Particle count Test 4. Recovery Test 5. Pressure balancing Test, 6. Air flow Pattern Test